|
Decarboxylation is any chemical reaction in which a carboxyl group (-COOH) is split off from a compound as carbon dioxide (CO2).
In biochemistry
Common biosynthetic decarboxylations of amino acids to amines are:
Other decarboxylation reactions from the citric acid cycle include:
Enzymes that catalyze decarboxylations are called decarboxylases or, more formally, carboxy-lyases (EC number 4.1.1).
In organic chemistry
In retrosynthesis, decarboxylation reactions can be considered the opposite of homologation reactions, in that the chain length becomes one carbon shorter.
Chemical decarboxylations reactions often require extensive heating in high-boiling solvents. Copper salts are often added as catalysts. Heating a carboxylic acid strongly with soda lime is also able to effect decarboxylation.[1] Heating the product of the malonic ester synthesis with hydrochloric acid also affords decarboxylation.[2] The addition of catalytic amounts of cyclohexen-2-one has been reported to catalyze the decarboxylation of amino acids.[citation needed]
Decarboxylations are especially easy for beta-keto acids due to the formation of a cyclic transition state for instance in Knoevenagel condensations.[citation needed] The Barton decarboxylation and Hunsdiecker reaction are radical reactions.
Kolbe electrolysis — the electrolysis of salts of carboxylic acids give the decarboxylated dimer products:
- CH3COOH ? CH3COO- ? CH3COO· ? CH3· + CO2
- 2CH3· ? CH3CH3
This reaction occurs via a radical mechanism as well.[3]
See also
References
- ^ Jim Clark (2004). "The Decarboxylation of Carboxylic Acids and their Salts". Chemguide. Retrieved on 2007-10-22.
- ^ "Malonic Ester Synthesis". Organic Chemistry Portal. Retrieved on 2007-10-26.
- ^ "Kolbe Electrolysis". Organic Chemistry Portal. Retrieved on 2007-10-22.
| 
